view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7773): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0216 | 1 | 25 | 0.0400 | 7780 | c.110 others(7799): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7773): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0005 | a0005c0032 | a0005c0032t0005 | a0005c0032t0005g0138 | 1 | 25 | 0.0400 | 7780 | c.110 others(7799): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7773): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0010 | a0010c0010 | a0010c0010t0007 | a0010c0010t0007g0002 | 1 | 25 | 0.0400 | 7780 | c.110 others(7799): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7773): Show |
intron_variant | MODIFIER | HG01106.hp1 HG03098.hp2 |
a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0233 a0001c0009t0001g0234 |
2 | 26 | 0.0769 | 7780 | c.110 others(7799): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7774): Show |
intron_variant | MODIFIER | NA19030.hp2 NA19043.hp2 |
a0001 | a0001c0012a0001c0030 | a0001c0012t0001a0001c0030t0001 | a0001c0012t0001g0231 a0001c0030t0001g0232 |
2 | 26 | 0.0769 | 7781 | c.110 others(7800): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7775): Show |
intron_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0038 | 1 | 25 | 0.0400 | 7782 | c.110 others(7801): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7776): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0042 | 1 | 25 | 0.0400 | 7783 | c.110 others(7802): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7776): Show |
intron_variant | MODIFIER | HG02886.hp1 HG03225.hp2 |
a0001a0009 | a0001c0001a0009c0013 | a0001c0001t0002a0009c0013t0001 | a0001c0001t0002g0044 a0009c0013t0001g0041 |
2 | 26 | 0.0769 | 7783 | c.110 others(7802): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7776): Show |
intron_variant | MODIFIER | HG01243.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
a0001 | a0001c0001a0001c0019a0001c0043 | a0001c0001t0002a0001c0019t0011a0001c0043t0002 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(7): Show |
10 | 34 | 0.2941 | 7783 | c.110 others(7802): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7776): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0054 | 1 | 25 | 0.0400 | 7783 | c.110 others(7802): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7776): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0009 | a0009c0013 | a0009c0013t0001 | a0009c0013t0001g0043 | 1 | 25 | 0.0400 | 7783 | c.110 others(7802): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7776): Show |
intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0058 | 1 | 25 | 0.0400 | 7783 | c.110 others(7802): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7776): Show |
intron_variant | MODIFIER | HG02559.hp1 HG02622.hp1 |
a0001 | a0001c0002 | a0001c0002t0014 | a0001c0002t0014g0132 a0001c0002t0014g0133 |
2 | 26 | 0.0769 | 7783 | c.110 others(7802): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7776): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0167 | 1 | 25 | 0.0400 | 7783 | c.110 others(7802): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7776): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0174 | 1 | 25 | 0.0400 | 7783 | c.110 others(7802): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7776): Show |
intron_variant | MODIFIER | HG01069.hp2 HG01169.hp1 HG02145.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0154 a0001c0001t0001g0171 a0001c0001t0001g0191 |
3 | 27 | 0.1111 | 7783 | c.110 others(7802): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG03041.hp1 NA18522.hp2 |
a0012 | a0012c0018 | a0012c0018t0001 | a0012c0018t0001g0213 a0012c0018t0001g0214 |
2 | 26 | 0.0769 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0009 | a0009c0013 | a0009c0013t0001 | a0009c0013t0001g0040 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0048 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0019 | a0001c0019t0011 | a0001c0019t0011g0053 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0026 | a0026c0022 | a0026c0022t0003 | a0026c0022t0003g0011 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0013 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG02976.hp1 HG03209.hp2 NA20129.hp2 |
a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0008 a0001c0004t0003g0009 a0001c0004t0003g0010 |
3 | 27 | 0.1111 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG01257.hp1 HG01258.hp2 |
a0001 | a0001c0021 | a0001c0021t0001 | a0001c0021t0001g0156 a0001c0021t0001g0172 |
2 | 26 | 0.0769 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG01361.hp2 | a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0195 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | NA18999.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0194 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0134 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG01123.hp2 HG01516.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0175 a0001c0001t0001g0181 |
2 | 26 | 0.0769 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG00741.hp2 HG01109.hp2 HG01516.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0028 others(3): Show |
6 | 30 | 0.2000 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00741.hp1 others(11): Show |
a0001a0004 | a0001c0001a0004c0007 | a0001c0001t0001a0001c0001t0004a0004c0007t0001 | a0001c0001t0001g0032 a0001c0001t0001g0135 a0001c0001t0001g0146 others(11): Show |
14 | 38 | 0.3684 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0179 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | HG02083.hp1 NA18959.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | 26 | 0.0769 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7777): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0142 | 1 | 25 | 0.0400 | 7784 | c.110 others(7803): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02055.hp2 |
a0001a0015 | a0001c0004a0015c0025 | a0001c0004t0003a0015c0025t0003 | a0001c0004t0003g0012 a0015c0025t0003g0006 |
2 | 26 | 0.0769 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0007 | 1 | 25 | 0.0400 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG01123.hp1 HG01978.hp2 HG02074.hp1 others(2): Show |
a0001a0017a0022 | a0001c0001a0017c0037a0022c0040 | a0001c0001t0001a0017c0037t0001a0022c0040t0001 | a0001c0001t0001g0164 a0001c0001t0001g0166 a0001c0001t0001g0222 others(2): Show |
5 | 29 | 0.1724 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0223 | 1 | 25 | 0.0400 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0159 | 1 | 25 | 0.0400 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0042 | a0001c0042t0001 | a0001c0042t0001g0180 | 1 | 25 | 0.0400 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG02738.hp2 | a0004 | a0004c0007 | a0004c0007t0001 | a0004c0007t0001g0144 | 1 | 25 | 0.0400 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG00738.hp1 | a0014 | a0014c0038 | a0014c0038t0001 | a0014c0038t0001g0027 | 1 | 25 | 0.0400 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 | 1 | 25 | 0.0400 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00735.hp1 HG01168.hp1 others(5): Show |
a0001a0003 | a0001c0001a0003c0005 | a0001c0001t0001a0003c0005t0001 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0160 others(5): Show |
8 | 32 | 0.2500 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG04228.hp1 | a0004 | a0004c0007 | a0004c0007t0001 | a0004c0007t0001g0140 | 1 | 25 | 0.0400 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | NA19090.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0173 | 1 | 25 | 0.0400 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG02109.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
4 | 28 | 0.1429 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7778): Show |
intron_variant | MODIFIER | HG01993.hp2 | a0016 | a0016c0039 | a0016c0039t0001 | a0016c0039t0001g0186 | 1 | 25 | 0.0400 | 7785 | c.110 others(7804): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7779): Show |
intron_variant | MODIFIER | HG03041.hp2 | a0001 | a0001c0012 | a0001c0012t0012 | a0001c0012t0012g0218 | 1 | 25 | 0.0400 | 7786 | c.110 others(7805): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DMXL1_chr5_119066087_119254127 | 119123748 | G | GGCCTCCC others(7779): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0005 | 1 | 25 | 0.0400 | 7786 | c.110 others(7805): Show |
DMXL1 | ENSG00000172869.15 | transcript | ENST00000539542.6 | protein_coding | 9/43 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |